美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
0093-8739-01	0093-8739	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	19950605	N/A	ANDA	ANDA074377	Teva Pharmaceuticals USA, Inc.	MEXILETINE HYDROCHLORIDE	150 mg/1	100 CAPSULE in 1 BOTTLE (0093-8739-01)
42291-626-01	42291-626	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20130709	N/A	ANDA	ANDA074377	AvKARE	MEXILETINE HYDROCHLORIDE	250 mg/1	100 CAPSULE in 1 BOTTLE (42291-626-01)
42291-624-01	42291-624	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20130709	N/A	ANDA	ANDA074377	AvKARE	MEXILETINE HYDROCHLORIDE	150 mg/1	100 CAPSULE in 1 BOTTLE (42291-624-01)
0093-8740-01	0093-8740	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	19950605	N/A	ANDA	ANDA074377	Teva Pharmaceuticals USA, Inc.	MEXILETINE HYDROCHLORIDE	200 mg/1	100 CAPSULE in 1 BOTTLE (0093-8740-01)
42291-625-01	42291-625	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20130709	N/A	ANDA	ANDA074377	AvKARE	MEXILETINE HYDROCHLORIDE	200 mg/1	100 CAPSULE in 1 BOTTLE (42291-625-01)
0093-8741-01	0093-8741	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	19950605	N/A	ANDA	ANDA074377	Teva Pharmaceuticals USA, Inc.	MEXILETINE HYDROCHLORIDE	250 mg/1	100 CAPSULE in 1 BOTTLE (0093-8741-01)